Perinatal Depression Clinical Trial
— MInD-IOfficial title:
Remote Supervision for Implementing Collaborative Care for Perinatal Depression
Verified date | April 2021 |
Source | University of Washington |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study evaluates the impact of a longitudinal remote consultation (LRC) implementation strategy for collaborative care depression treatment among perinatal women. All participating health centers will receive training in collaborative care. Cluster randomization will be used to assign the addition of LRC to select health centers. Differences in implementation success, clinical outcomes, and costs will be compared after a 12 month implementation period and 13-21 month sustainment period.
Status | Active, not recruiting |
Enrollment | 20 |
Est. completion date | July 2021 |
Est. primary completion date | July 2021 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 45 Years |
Eligibility | Patient Participants: Inclusion Criteria: - Patient participants must be perinatal women, - Age 18-45, - Receiving care at one of the 20 OCHIN or non-OCHIN health centers participating in the study and must have major depression as determined by a score of =10 on the PHQ-9 depression screener. Exclusion Criteria: - Age <18 or >45, - Male. Health Center Participating Sites: Inclusion Criteria: - Use of the shared OCHIN Epic electronic record for perinatal care or use of the secure AIMS CMTS/Caseload Tracker/spreadsheet patient registry for perinatal care and - A minimum of 50 prenatal patients annually. |
Country | Name | City | State |
---|---|---|---|
United States | University of Washington | Seattle | Washington |
Lead Sponsor | Collaborator |
---|---|
University of Washington | National Institute of Mental Health (NIMH), Ochin, Inc., Oregon Social Learning Center, University of Pennsylvania, Washington University School of Medicine |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Cost and cost-effectiveness | For a cost-benefit analysis, the investigators will use of the Cost of Implementing New Strategies (COINS) method to assess costs in the two conditions. This methodology takes advantage of the SIC-CC instrument as a costing template to map the use of resources and associated costs to these to study conditions. Costs associated with implementation in each of these conditions will be carried out for all 20 health centers included in the study. | 12-month post-implementation of collaborative care | |
Primary | Clinical depression outcomes | Patient Health Questionnaire-9 (PHQ-9); level of depression symptomatology and functional impairment. | 12 months post-initiation of collaborative care | |
Secondary | Implementation outcomes | To assess the degree to which sites in the two conditions complete implementation, the investigators will use the Stages of Implementation Completion tool tailored for collaborative care, SIC-CC. | 12 month post-implementation of collaborative care |
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